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THOMAS JAMISON, MD

MD

Integrative Medicine Physician

NPI: 1962476077Individual

Specialties, Licenses & Credentials

Internal Medicine Physician

Internal Medicine

Code: 207R00000X

2024-00797(NC)2019005174(MO)036.156348(IL)0101047305(VA)
Integrative Medicine PhysicianPrimary

Integrative Medicine

Code: 202D00000X

2024-00797(NC)

Research & Publications (20)

Water overcomes methyl group directing effects in epoxide-opening cascades.
PMID 19402635·J Am Chem Soc·2009
8-other
Epoxide-opening cascades in the synthesis of polycyclic polyether natural products.
PMID 19572302·Angew Chem Int Ed Engl·2009
6-review
Functionalized templates for the convergent assembly of polyethers: synthesis of the HIJK rings of gymnocin A.
PMID 19431181·Angew Chem Int Ed Engl·2009
8-other
Mechanism and transition-state structures for nickel-catalyzed reductive alkyne-aldehyde coupling reactions.
PMID 19397371·J Am Chem Soc·2009
8-other
Macrocyclization by nickel-catalyzed, ester-promoted, epoxide-alkyne reductive coupling: total synthesis of (-)-gloeosporone.
PMID 19536804·Angew Chem Int Ed Engl·2009
8-other
On the synergism between H2O and a tetrahydropyran template in the regioselective cyclization of an epoxy alcohol.
PMID 19385615·J Am Chem Soc·2009
8-other
Total synthesis of ent-dioxepandehydrothyrsiferol via a bromonium-initiated epoxide-opening cascade.
PMID 19663441·J Am Chem Soc·2009
8-other
The pharmacodynamic properties of azithromycin in a kinetics-of-kill model and implications for bacterial conjunctivitis treatment.
PMID 18369536·Adv Ther·2008
8-other
Alpha-olefins as alkenylmetal equivalents in catalytic conjugate addition reactions.
PMID 18236501·Angew Chem Int Ed Engl·2008
8-other
SmI2-promoted Reformatsky-type coupling reactions in exceptionally hindered contexts.
PMID 18302397·Org Lett·2008
8-other
Ocular distribution, bactericidal activity and settling characteristics of TobraDex ST ophthalmic suspension compared with TobraDex ophthalmic suspension.
PMID 18309465·Adv Ther·2008
4-observational
Epoxide-opening cascades promoted by water.
PMID 17761875·Science·2007
7-preclinical
Regioselectivity and enantioselectivity in nickel-catalysed reductive coupling reactions of alkynes.
PMID 17971951·Chem Commun (Camb)·2007
8-other
Total synthesis of pumiliotoxins 209F and 251D via late-stage, nickel-catalyzed epoxide-alkyne reductive cyclization.
PMID 17696401·J Org Chem·2007
8-other
Nickel-catalyzed synthesis of acrylamides from alpha-olefins and isocyanates.
PMID 17269783·Org Lett·2007
8-other
Total synthesis of (+)-acutiphycin.
PMID 17985925·J Org Chem·2007
8-other
Highly selective coupling of alkenes and aldehydes catalyzed by [Ni(NHC){P(OPh)3}]: synergy between a strong sigma donor and a strong pi acceptor.
PMID 17154217·Angew Chem Int Ed Engl·2007
8-other
trans-hydroalumination/alkylation: one-pot synthesis of trisubstituted allylic alcohols.
PMID 16898811·Org Lett·2006
8-other
Nickel-catalyzed coupling of alkenes, aldehydes, and silyl triflates.
PMID 16939275·J Am Chem Soc·2006
8-other
Highly convergent total synthesis of (+)-acutiphycin.
PMID 17117859·J Am Chem Soc·2006
8-other

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
1690 US HIGHWAY 1 S, SUITE 300
SOUTHERN PINES, NC 28387

Location

Practice Location

1690 US HIGHWAY 1 S, SOUTHERN PINES, NC
(910) 684-5499

Quick Facts

NPI
1962476077
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
5
Locations
1
Publications
20

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